Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, India.
Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, India.
Exp Neurol. 2021 Jun;340:113656. doi: 10.1016/j.expneurol.2021.113656. Epub 2021 Feb 24.
Heat shock response (HSR) is a conserved cytoprotective pathway controlled by the master transcriptional regulator, the heat shock factor 1 (HSF1), that activates the expression of heat shock proteins (HSPs). HSPs, as chaperones, play essential roles in minimizing stress-induced damages and restoring proteostasis. Therefore, compromised HSR is thought to contribute to neurodegenerative disorders. Lafora disease (LD) is a fatal form of neurodegenerative disorder characterized by the accumulation of abnormal glycogen as Lafora bodies in neurons and other tissues. The symptoms of LD include progressive myoclonus epilepsy, dementia, and cognitive deficits. LD is caused by the defects in the gene coding laforin phosphatase or the malin ubiquitin ligase. Laforin and malin are known to work upstream of HSF1 and are essential for the activation of HSR. Herein, we show that mice deficient for laforin or malin show reduced levels of HSF1 and their targets in their brain tissues, suggesting compromised HSR; this could contribute to the neuropathology in LD. Intriguingly, treatment of LD animals with dexamethasone, a synthetic glucocorticoid analogue, partially restored the levels of HSF1 and its targets. Dexamethasone treatment was also able to ameliorate the neuroinflammation and susceptibility to induced seizures in the LD animals. However, dexamethasone treatment did not show a significant effect on Lafora bodies or autophagy defects. Taken together, the present study establishes a role for HSR in seizure susceptibility and neuroinflammation and dexamethasone as a potential antiepileptic agent, suitable for further studies in LD.
热休克反应 (HSR) 是一种保守的细胞保护途径,由主转录调节因子热休克因子 1 (HSF1) 控制,该因子激活热休克蛋白 (HSPs) 的表达。HSPs 作为伴侣蛋白,在最小化应激诱导的损伤和恢复蛋白质平衡方面发挥着重要作用。因此,HSR 受损被认为是导致神经退行性疾病的原因之一。拉佛拉病 (LD) 是一种致命的神经退行性疾病,其特征是神经元和其他组织中异常糖原为拉佛拉体的积累。LD 的症状包括进行性肌阵挛癫痫、痴呆和认知缺陷。LD 是由编码 laforin 磷酸酶或 malin 泛素连接酶的基因缺陷引起的。已知 laforin 和 malin 在 HSF1 的上游起作用,是 HSR 激活所必需的。在此,我们表明,laforin 或 malin 缺失的小鼠其脑组织中 HSF1 及其靶标水平降低,提示 HSR 受损;这可能导致 LD 中的神经病理学。有趣的是,用合成糖皮质激素类似物地塞米松治疗 LD 动物部分恢复了 HSF1 及其靶标的水平。地塞米松治疗还能够改善 LD 动物的神经炎症和易发性癫痫。然而,地塞米松治疗对拉佛拉体或自噬缺陷没有显著影响。综上所述,本研究确立了 HSR 在癫痫易感性和神经炎症中的作用,以及地塞米松作为一种潜在的抗癫痫药物,适合在 LD 中进一步研究。